Electrolytic solution and electrochemical cell using the same

ABSTRACT

The present invention relates to an electrolytic solution comprising an aqueous solution of an organic or inorganic acid whereto a water-soluble N-containing heterocyclic compound is added, and an electrochemical cell such as a secondary battery and an electric double layer capacitor that uses such an electrolytic solution.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to an electrolytic solution used in anelectrochemical cell such as a secondary battery and an electric doublelayer capacitor, and an electrochemical cell such as a secondary batteryand an electric double layer capacitor that uses such an electrolyticsolution; more specifically the present invention relates to anelectrolytic solution to prevent the oxidation and degradation ofelectrode active materials, and to improve the cycle properties in acell that includes a proton-conducting polymer as an active material.

2. Related Art

An electrochemical cell, such as a secondary battery and an electricdouble layer capacitor, that uses a proton-conducting polymer as anelectrode active material (hereafter referred to as “cell”) has beenproposed and put to practical use. Such a cell has a constitution, forexample as shown in FIG. 1, wherein a positive electrode 2 containing aproton-conducting polymer as the active material on a positive electrodecollector 1, a negative electrode 4 on a negative electrode collector 3,and these are laminated via a separator 5; and only protons involve aselectric charge carriers. An aqueous or non-aqueous solution containinga proton source is filled as an electrolytic solution. Reference numeral6 denotes a gasket.

The electrodes are formed on collectors, such as a conductive rubbersheets, by slurry prepared from the powder of a doped or non-dopedmaterial polymer (proton-conducting polymer), a conducting additive, anda binder, which is put in a mold of a desired size and compressed with ahot press to have desired electrode density and film thickness. Thusformed positive electrode and negative electrode are arranged so as toface each other through a separator to constitute a cell.

Proton-conducting polymers used as electrode active materials includeπ-conjugated polymers, such as polyaniline, polythiophene, polypyrrole,polyacetylene, poly-p-phenylene, polyphenylenevinylene,polyperinaphthalene, polyfuran, polyfurfuran, polythienylene,polypyridinediyl, polyisothianaphthene, polyquinoxaline, polypyridine,polypyrimidine, polyindole, indole trimer, polyaminoanthraquinone, andderivatives thereof; and polymers containing hydroxyl groups (formedfrom quinone oxygen due to conjugation), such as polyanthraquinone andpolybenzoquinone. Redox pairs are formed by doping an appropriate dopantto these polymers, and conductivity appears. By adequately adjustingoxidation-reduction potential difference, these polymers are selectedand used as active materials for positive and negative electrodes.

As the electrolytic solution, an aqueous electrolytic solutioncomprising an aqueous solution of an acid, and a non-aqueouselectrolytic solution based on an organic solvent have been known, andin proton-conducting polymers, the former aqueous electrolytic solutionis exclusively used because the cell of a particularly high capacity canbe provided. The acids include inorganic acids, such as sulfuric acid,nitric acid, hydrochloric acid, phosphoric acid, tetrafluoroboric acid,and hexafluosilicic acid; and organic acids, such as saturatedmonocarboxylic acids, aliphatic carboxylic acids, oxycarboxylic acids,p-toluene sulfonic acid, polyvinyl sulfonic acid, and lauric acid.

In a cell using such proton-conducting polymers as active materials, thecycle life is shortened by the rise of internal resistance, and thistendency becomes significant with the elevation of temperature. There isa problem of the degradation of long-term stability in ahigh-temperature atmosphere.

The causes are that the progress of proton adsorption-desorptionreaction, which is the charge-discharge mechanism of electrode activematerials, is deteriorated, the degrading atmosphere increases, theexcessive oxidation of the materials is accelerated especially in hightemperatures, and therefore, the progress of degradation increases. Itis also the cause that the heat stability of the electrolytic solutionis insufficient.

Particularly, the active materials for electrodes are easily degradedunder oxidizing conditions. This is considered to be caused bydegradation of the proton (H⁺) adsorption-desorption reaction of activematerial compounds over time in the charge-discharge mechanism asdescribed below. The contributing factors include the progress ofdegradation of active materials in an excessive H⁺ concentrationatmosphere compared with an optimal H⁺ concentration (different betweenactive materials and depending on the number of reactive electrons),whereby doping-dedoping reactivity between the active material and theelectrolyte lowers, and reaction cannot proceed smoothly, andcharge-discharge ability lowers (called “excessive oxidationdegradation”).

Here, an indole-based polymer (indole trimer) used as the activematerial for a positive electrode, and a quinoxaline-based polymer usedas the active material for a negative electrode will be described.

The charge-discharge mechanism of the materials for positive andnegative electrodes is shown in the following scheme:

where R represents an optional substituent group, and X represents ananion.

Since this phenomenon is especially significant in a high acidconcentration atmosphere (low pH), the degradation of the cycleproperties is accelerated. Also, since the conductivity of theelectrolyte increases, and the reaction with the active material isactivated in a high temperature atmosphere, the progress of degradationby oxidation may be enhanced if the concentration of the electrolyte isexcessive.

FIG. 2 is a graph showing change in cycle properties by theconcentration of the electrolyte (sulfuric acid). As the graph shows, itcan be seen that with increase in the concentration of the electrolyte,the capacity ratio lowers in larger number of cycles, and the cycleproperties are degraded.

In an atmosphere of low-concentration of the electrolyte, although thecycle properties are satisfactory, the appearance capacities tend tolower. FIG. 3 is a graph showing change in the appearance capacities bythe concentration of the electrolyte (sulfuric acid). As the graphshows, it can be seen that with decrease in the concentration of theelectrolyte, the appearance capacities lower.

Therefore, the establishment of the optimal composition of theelectrolyte (H⁺ and X⁻) is required, and this is the problem to improvethe cycle properties.

SUMMARY OF THE INVENTION

The object of the present invention is to prevent the degradation by theoxidation of the active materials for electrodes, and to improve thecycle properties, without lowering appearance capacities in the cellcontaining a proton-conducting polymer as the active material.

The present inventors carried out repeated studies to solve theabove-described problems, and found that the cell with improved cycleproperties can be provided without lowering the appearance capacities,by adding a specific substance to the electrolytic solution filled inthe cell. That is, the present invention is an electrolytic solutioncomprising an aqueous solution of an organic or inorganic acid whereto awater-soluble N-containing heterocyclic compound is added.

Also, the present invention is the electrolytic solution wherein thewater-soluble N-containing heterocyclic compound is at least onecompound selected from imidazole and the derivatives thereof representedby the following formula (1); triazoles and the derivatives thereofrepresented by the following formula (2) or (3); and pyrazole and thederivatives thereof represented by the following formula (4):

where R represents individually and independently a hydrogen atom, analkyl group having 1 to 4 carbon atoms, an amino group, a carboxylgroup, a nitro group, a phenyl group, a vinyl group, a halogen atom, anacyl group, a cyano group, a trifluoromethyl group, an alkyl sulfonylgroup, or a trifluoromethylthio group.

It is preferable that the water-soluble N-containing heterocycliccompound is contained in the proportion of 1 to 80% by weight to 100% byweight of an electrolyte.

Also, the present invention relates to an electrochemical cell, such asa secondary battery and an electric double layer capacitor, comprising apositive electrode and a negative electrode facing each other in anelectrolytic solution via a separator and a proton-conductive polymer,which is an active material of an electrode in the positive electrodeand in the negative electrode in which only a proton participates in acharge/discharge, wherein the above-described electrolytic solution isused as the electrolytic solution.

By the use of the electrolytic solution of the present invention, asdescribed above, the cycle properties have been improved withoutlowering appearance capacities. This is because the N-containingheterocyclic compound added to the electrolytic solution absorbs protonsin the electrolytic solution, and makes the proton concentration in theelectrolytic solution lower than the anion concentration, enabling thedegradation of the active materials of electrodes by oxidation to beinhibited.

The use of the electrolytic solution of the present invention has theeffect of improving the self-discharge properties and the withstandvoltage properties. This is considered because a cation isresonance-stabilized by delocalization of the N-containing heterocycliccompound added to the electrolytic solution, and interacts with an anionin the electrolytic solution caused by electrochemical decomposition,inhibiting the production of gas due to the electrolysis of theelectrolytic solution, and improving thermal stability of theelectrolytic solution.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a sectional view showing an example of an electrochemical cellaccording to the present invention.

FIG. 2 is a graph showing change in cycle properties of a conventionalelectrochemical cell due to difference in the concentration of sulfuricacid.

FIG. 3 is a graph showing change in appearance capacities of aconventional electrochemical cell due to difference in the concentrationof sulfuric acid.

FIG. 4 is a graph showing the results of CV measurement ofpositive-electrode active materials in the electrolytic solutionaccording to the present invention and a conventional electrolyte.

FIG. 5 is a graph showing the results of CV measurement ofnegative-electrode active materials in the electrolytic solutionaccording to the present invention and a conventional electrolyte.

FIG. 6 is a graph showing change in cycle properties of cells using theelectrolytic solutions according to the present invention (Examples 2and 6) and the electrolytic solutions according to conventional examples(Comparative Examples 1 and 2).

FIG. 7 is a graph showing the results of the self-discharge propertytests of cells using the electrolytic solutions according to the presentinvention (Examples 2 and 6) and the electrolytic solutions according toconventional examples (Comparative Examples 1 and 2).

FIG. 8 is a graph showing the results of the withstand voltage tests ofcells using the electrolytic solutions according to the presentinvention (Examples 2 and 6) and the electrolytic solutions according toconventional examples (Comparative Examples 1 and 2).

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

The present invention will be described in detail below.

The present invention is characterized in that a water-solubleN-containing heterocyclic compound is added to the electrolytic solutionin order to control the ion concentration in the electrolytic solutionthat contributes to the doping-dedoping reaction. It is considered thatthe addition of the N-containing heterocyclic compound causes thefollowing interactions. Here, the N-containing heterocyclic compound isexemplified by imidazole.

where n represents the concentration of imidazole, Y represents theconcentration of the electrolyte, and X represents an anion.

As the above formula shows, imidazole adsorbs protons, the compositionof the aqueous solution of the acid becomes (Y-n)H⁺ and XY⁻, and thequantity of protons in the electrolytic solution becomes less than thequantity of anions. As a result, the excessive oxidation of the activematerials (for positive and negative electrodes) is prevented, and thecycle life is elongated. Thus, the concentration of anions to be adopant does not change, and the concentration of protons can be adjustedas desired by controlling the quantity of the added N-containingheterocyclic compound. Thereby, the improvement of cycle properties canbe realized while maintaining high appearance capacities.

Non-aqueous electrolytic solutions whereto an N-containing heterocycliccompound are disclosed in Japanese Patent Laid-Open Nos. 2000-156329 and2001-143748.

Disclosed in Japanese Patent Laid-Open No. 2000-156329 is an electrolytefor aluminum electrolytic capacitors comprising a cation of aquaternized compound having N,N,N′-substituted amidine groups, and anorganic acid anion in an organic solvent. While a conventionalelectrolytic solution using a quaternary ammonium salt of a carboxylicacid accelerates the degradation of a rubber sealant, and lowers thesealing performance significantly, the thermal stability and thespecific conductivity of the electrolytic solution are improved by theaddition of the cationic quaternary amidine. Particularly in a compoundresulting from resonance stabilization of the cation due to electrondelocalization in the amidine group, a high specific conductivity ispresumably obtained by the promotion of ionic dissociation. Furthermore,when excessive hydroxide ions are produced as a result of theelectrolysis reaction in the electrolytic solution, the hydroxide iondisappears rapidly owing to its reaction with the amidine group, andtherefore, the effect of the electrolytic reaction can be minimizedunlike conventional amines such as quaternary ammonium salts. As aresult, the degradation of the sealant of the capacitor can beprevented, and the sealing performance can be enhanced.

On the other hand, disclosed in Japanese Patent Laid-Open No.2001-143748 is an electrolytic solution used in non-aqueous electrolytelithium secondary batteries, wherein a lithium salt of a perfluoroalkylsulfonic acid derivative is dissolved in an organic solvent, and ischaracterized in containing at least one compound selected fromheterocyclic compounds having one or more fluorine atom, and containingnitrogen or oxygen. In this reference, the heterocyclic compound addedto the electrolytic solution forms a film of a strong adsorbing layerhaving resistance against the oxidation of the positive electrodecollector on the positive electrode collector, to inhibit thedegradation of the positive electrode collector by oxidation, and toimprove the cycle properties.

The above-described two prior art techniques use non-aqueouselectrolytic solutions, and differ from the aqueous electrolyticsolution of the present invention. The reaction mechanism of thesenon-aqueous electrolytic solutions is entirely different from thedegradation of the active materials for electrodes by oxidation of thecell using a proton-conducting polymer of the present invention, and inno way teaches anything to the present invention.

Next, in order to verify the effect for the prevention of degradation ofthe active materials, cyclic voltammmetry (CV) measurement was carriedout on the active materials for the positive electrode (indol trimer) inthe electrolytic solution of the present invention. In the measurement,the films of active materials for the positive electrode and thenegative electrode formed on carbon sheets were used as workingelectrodes, platinum was used as the counter electrode, and an Ag/AgClelectrode was used as the reference electrode. The measurementtemperature was 25° C., the scanning potential was 600 to 1100 mV, andthe scanning speed was 1 mV/sec. The composition of Example 2, describedlater, that is, a 20% by weight aqueous solution of sulfuric acidwhereto 20% by weight of imidazole to 100% by weight of sulfuric acidwas dissolved was used as an electrolytic solution. For reference, theexample whereto imidazole was not added (Comparative Example 1 describedlater) was also evaluated. The results are shown in FIG. 4.

As a result, the oxidation-reduction potential shifted to thelow-potential side by several tens of millivolts, i.e., stablepotential, which is the direction to relax degradation by oxidation.

Similarly, the CV measurement was carried out on the active material forthe negative electrode (polyphenyl quinoxaline), and change in thedischarge capacity was measured. The results are shown in FIG. 5. Theseresults showed that the degradation of not only the positive electrode,but also the negative electrode can be prevented.

In the electrolytic solution of the present invention, since pH changesaccompanying the concentration of the added N-containing heterocycliccompound, the oxidation decomposition potential and the gas generationpotential shift, and within the working voltage range of batteries(rating: 1.2 V/cell), the electrolytic solution having a sufficientlyhigh electrical stability can be obtained.

In an N-containing heterocyclic compound, such as imidazole, electronsare delocalized on —N═C—N— in the ring thereof, and cations areresonance-stabilized as described below. It is considered that theresonance-stabilized cations interact with —OH⁻ and —X⁻ produced byelectrochemical decomposition, and has the effect to inhibit thegeneration of gas by the electrolysis of the electrolyte. Furthermore,the thermal stability of the electrolytic solution is also improved.

Since the present invention is an aqueous electrolytic solution, it isessential that the added N-containing heterocyclic compound iswater-soluble. Although the number of nitrogen atoms in the ring is notlimited, especially preferable compounds are at least one compoundselected from imidazole and the derivatives thereof represented by thefollowing formula (1); triazoles and the derivatives thereof representedby the following formula (2) or (3); and pyrazole and the derivativesthereof represented by the following formula (4). These N-containingheterocyclic compounds may be used alone, or may be the mixture of morethan one.

where R represents individually and independently a hydrogen atom, analkyl group having 1 to 4 carbon atoms, an amino group, a carboxylgroup, a nitro group, a phenyl group, a vinyl group, a halogen atom, anacyl group, a cyano group, a trifluoromethyl group, an alkyl sulfonylgroup, or a trifluoromethylthio group.

Any proton-conducting polymers exemplified in the description of priorart can be used as the active materials for electrodes constituting thecell of the present invention. Preferably, the active materials forpositive electrodes are selected from the group consisting ofpolyaniline, polydianiline, polydiaminoanthraquinone,polybiphenylaniline, polynaphthylaniline, indole trimer, and thederivatives thereof; and the active materials for negative electrodesare selected from the group consisting of polypyridine, polypyrimidine,polyquinoxaline, and the derivatives thereof. The particularlypreferable is the combination of indole trimer andpolyphenylquinoxaline.

The electrolyte containing in the electrolytic solution can be organicor inorganic acids described in the prior art, and the particularlypreferable is sulfuric acid.

The quantity of the N-containing heterocyclic compounds added to theelectrolytic solution can be selected optionally and is not limited tospecific quantity; however, if the quantity is excessively small, theeffect of preventing the degradation of active materials by oxidationmay be small. On the contrary, if the quantity is excessively large, theappearance capacity may lower due to the elevation of pH, theconductivity of the electrolyte may lower (due to the elevation of pH),and other properties may also be deteriorated. Although it depends onthe kind and concentration of the electrolyte, and the kind of theadditives, the quantity of the N-containing heterocyclic compounds ispreferably about 1 to 80% by weight to 100% by weight of theelectrolyte.

The present invention will be described in detail below referring toexamples; however, the present invention is not limited only to theseexamples. Although the application to secondary cells in the followingexamples will be described, the present invention can also be applied tothe constitutions suitable for other electrochemical cells, such aselectric double layer capacitors, by adjusting the capacities and thecharge-discharge speed adequately.

EXAMPLE 1

As the positive electrode, a solid electrode formed from an indoletrimer as the active material whereto 20% by weight of vapor-phase growncarbon fiber (VGCF) was added as a conducting additive, and 8% by weightof polyvinylidene fluoride (average molecular weight: 1100) was added asan electrode binder, stirred and mixed in a blender, and molded into adesired size with a hot press, was used.

As the negative electrode, a solid electrode formed frompolyphenylquinoxaline as the active material whereto 25% by weight ofcarbon black (K.B. 600) was added as a conducting additive, stirred andmixed in a blender, and molded into a desired size with a hot press, wasused.

As the electrolytic solution, a 20% by weight (2.3 mol/L) aqueoussolution of sulfuric acid whereto 10% by weight (0.15 mol/L) ofimidazole to 100% by weight of sulfuric acid was dissolved as anadditive was used.

The above-described positive electrode and the negative electrode werebonded to face each other via a polyolefin-based porous film of athickness of 20 to 50 μm as a separator to form a battery of theconstitution shown in FIG. 1.

EXAMPLE 2

A battery was manufactured in the same manner as in Example 1 exceptthat a 20% by weight (2.3 mol/L) aqueous solution of sulfuric acidwhereto 30% by weight (0.45 mol/L) of imidazole to 100% by weight ofsulfuric acid was dissolved as an additive was used as the electrolyticsolution.

EXAMPLE 3

A battery was manufactured in the same manner as in Example 1 exceptthat a 20% by weight (2.3 mol/L) aqueous solution of sulfuric acidwhereto 50% by weight (0.75 mol/L) of imidazole to 100% by weight ofsulfuric acid was dissolved as an additive was used as the electrolyticsolution.

EXAMPLE 4

A battery was manufactured in the same manner as in Example 1 exceptthat a 20% by weight (2.3 mol/L) aqueous solution of sulfuric acidwhereto 30% by weight (0.45 mol/L) of triazole to 100% by weight ofsulfuric acid was dissolved as an additive was used as the electrolyticsolution.

EXAMPLE 5

A battery was manufactured in the same manner as in Example 1 exceptthat a 20% by weight (2.3 mol/L) aqueous solution of sulfuric acidwhereto 30% by weight (0.45 mol/L) of pyrazole to 100% by weight ofsulfuric acid was dissolved as an additive was used as the electrolyticsolution.

EXAMPLE 6

A battery was manufactured in the same manner as in Example 1 exceptthat a 20% by weight (2.3 mol/L) aqueous solution of sulfuric acidwhereto 15% by weight (0.225 mol/L) of imidazole and 15% by weight(0.225 mol/L) of triazole to 100% by weight of sulfuric acid wasdissolved as an additive was used as the electrolytic solution.

EXAMPLE 7

A battery was manufactured in the same manner as in Example 1 exceptthat a 20% by weight (2.3 mol/L) aqueous solution of sulfuric acidwhereto 30% by weight (0.45 mol/L) of 3-trifluoromethyl-pyrazole to 100%by weight of sulfuric acid was dissolved as an additive was used as theelectrolytic solution.

EXAMPLE 8

A battery was manufactured in the same manner as in Example 1 exceptthat a 25% by weight (3.0 mol/L) aqueous solution of sulfuric acidwhereto 78% by weight (1.15 mol/L) of imidazole to 100% by weight ofsulfuric acid was dissolved as an additive was used as the electrolyticsolution.

COMPARATIVE EXAMPLE 1

A battery was manufactured in the same manner as in Example 1 exceptthat a 20% by weight (2.3 mol/L) aqueous solution of sulfuric acid wasused as the electrolytic solution.

COMPARATIVE EXAMPLE 2

A battery was manufactured in the same manner as in Example 1 exceptthat a 25% by weight (3.0 mol/L) aqueous solution of sulfuric acid wasused as the electrolytic solution.

The appearance capacities, cycle properties, self-dischargingproperties, and withstand voltage properties of batteries manufacturedin Examples 1 to 8 and Comparative Examples 1 and 2 were evaluated. Theresults are shown in Table 1 below.

The appearance capacities were evaluated making the appearance capacityof comparative Example 1 as to 100%. The cycle properties are change incapacities after 10,000 cycles of the test (temperature in measurement:25° C.). The self-discharging properties are the capacity survival rateafter one month test (temperature in measurement: 25° C.). The withstandvoltage properties are change in the internal resistance after 1000hours of the rated voltage impressing test (temperature in measurement:60° C.).

The conditions of the cycle test were CCCV charging at 1 A and 1.2 V for10 minutes, CC discharging at 0.2 A, and the ending voltage of 0.8 V.

TABLE 1 Self- Withstand Appearance Cycle discharge voltage capacityproperty property property (%) (%) (%) (%) Example 1 99.9 89.2 82.4 108Example 2 99.2 93.3 88.9 105 Example 3 85.8 94.9 85.9 103 Example 4100.1 91.4 87.1 106 Example 5 99.9 90.2 86.2 107 Example 6 100.1 95.289.2 104 Example 7 97.8 89.1 83.3 109 Example 8 102.3 88.6 82.1 111Comparative 100.0 80.2 65.7 121 Example 1 Comparative 102.6 65.0 68.1138 Example 2

FIGS. 6 to 8 show the evaluation results of cycle properties, theself-discharge properties, and the withstand voltage properties ofExamples 2 and 6, and Comparative Examples 1 and 2, respectively.

It can be seen from the above results that the use of the electrolyticsolution of the present invention improves the cycle properties withoutlowering appearance capacities. It can be also seen that the use of theelectrolytic solution of the present invention has the effect ofimproving the self-discharge properties and the withstand voltageproperties.

Although the above-described examples use indole trimers andpolyphenylquinoxane as active materials, the present invention is notlimited thereto, but electrochemical cells using any proton-conductingpolymers can be applied.

1. An electrolytic solution comprising an electrolyte which is anorganic or inorganic acid, an additive which is a water-solubleN-containing heterocyclic compound, and a solvent which is water,wherein said water-soluble N-containing heterocyclic compound is atleast one compound selected from imidazole and the derivatives thereofrepresented by the following formula (1); triazoles and the derivativesthereof represented by the following formula (2) or (3); and pyrazoleand the derivatives thereof represented by the following formula (4):

where R represents individually and independently a hydrogen atom, analkyl group having 1 to 4 carbon atoms, an amino group, a carboxylgroup, a nitro group, a phenyl group, a vinyl group, a halogen atom, anacyl group, a cyano group, a trifluoromethyl group, an alkyl sulfonylgroup, or a trifluoromethylthio group.
 2. The electrolytic solutionaccording to claim 1, wherein the proportion of said water-solubleN-containing heterocyclic compound is 1 to 80% by weight to 100% byweight of the electrolyte in the electrolytic solution.
 3. Anelectrolytic solution comprising an electrolyte which is an organic orinorganic acid, an additive which is a water-soluble N-containingheterocyclic compound, and a solvent which is water, wherein saidwater-soluble N-containing heterocyclic compound is at least onecompound selected from imidazole and the derivatives thereof representedby the following formula (1); triazoles and the derivatives thereofrepresented by the following formula (2) or (3); and pyrazole and thederivatives thereof represented by the following formula (4):

where R represents individually and indenendently a hydrogen atom, analkyl group having 1 to 4 carbon atoms, an amino group, a carboxylgroup, a nitro group, a phenyl group, a vinyl group, a halogen atom, anacyl group, a cyano group, a trifluoromethyl group, an alkyl sulfonylgroup, or a trifluoromethylthio group, wherein said organic or inorganicacid is sulfuric acid.
 4. The electrolytic solution according to claim3, wherein the concentration of said sulfuric acid in the electrolyticsolution is 10 to 40% by weight.
 5. An electrochemical cell comprising apositive electrode and a negative electrode facing each other in anelectrolytic solution via a separator, and a proton-conductive polymer,which is an active material of an electrode in the positive electrodeand in the negative electrode in which only a proton participates in acharge/discharge, wherein an electrolytic solution comprising an aqueoussolution of an organic or inorganic acid whereto a water-solubleN-containing heterocyclic compound is added, is used as the electrolyticsolution.
 6. The electrochemical cell according to claim 5, wherein saidwater-soluble N-containing heterocyclic compound is at least onecompound selected from imidazole and the derivatives thereof representedby the following formula (1); triazoles and the derivatives thereofrepresented by the following formula (2) or (3); and pyrazole and thederivatives thereof represented by the following formula (4):

where R represents individually and independently a hydrogen atom, analkyl group having 1 to 4 carbon atoms, an amino group, a carboxylgroup, a nitro group, a phenyl group, a vinyl group, a halogen atom, anacyl group, a cyano group, a trifluoromethyl group, an alkyl sulfonylgroup, or a trifluoromethylthio group.
 7. The electrochemical cellaccording to claim 5, wherein the proportion of said water-solubleN-containing heterocyclic compound is 1 to 80% by weight to 100% byweight of an electrolyte in the electrolytic solution.
 8. Theelectrochemical cell according to claim 5, wherein said aqueous solutionof an acid contains sulfuric acid as an electrolyte.
 9. Theelectrochemical cell according to claim 8, wherein the concentration ofsaid sulfuric acid in the electrolytic solution is 10 to 40% by weight.10. The electrochemical cell according to claim 5, wherein saidelectrochemical cell is a proton-conducting secondary battery.
 11. Anelectrolytic solution in contact with an electrode made of aproton-conductive polymer, said solution comprising (i) a proton sourcewhich is an organic or inorganic acid, (ii) a proton-adsorption agentwhich is a water-soluble N-containing heterocyclic compound, and (iii) asolvent which is water, wherein said water-soluble N-containingheterocyclic compound is at least one compound selected from imidazoleand the derivatives thereof represented by the following formula (1);triazoles and the derivatives thereof represented by the followingformula (2) or (3); and pyrazole and the derivatives thereof representedby the following formula (4):

where R represents individually and independently a hydrogen atom, analkyl group having 1 to 4 carbon atoms, an amino group, a carboxylgroup, a nitro group, a phenyl group, a vinyl group, a halogen atom, anacyl group, a cyano group, a trifluoromethyl group, an alkyl sulfonylgroup, or a trifluoromethylthio group.